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2-Methylallyl Carbamate

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Identification
Molecular formula
C6H11NO2
CAS number
7747-34-6
IUPAC name
2-methylallyl carbamate
State
State

At room temperature, 2-Methylallyl carbamate is a liquid.

Melting point (Celsius)
-55.50
Melting point (Kelvin)
217.65
Boiling point (Celsius)
102.50
Boiling point (Kelvin)
375.65
General information
Molecular weight
115.14g/mol
Molar mass
115.1370g/mol
Density
0.9650g/cm3
Appearence

2-Methylallyl carbamate appears as a colorless to pale yellow liquid. The compound is often stored in a controlled environment to prevent decomposition and maintain its purity.

Comment on solubility

Solubility of 2-methylallyl carbamate

2-methylallyl carbamate, with the chemical formula C6H11NO2, exhibits interesting solubility characteristics that are important for various applications.

Key Aspects of Solubility:

  • Polar vs. Non-Polar: As an organic compound, 2-methylallyl carbamate presents a polar character due to the presence of the carbamate functional group (-NH2O). This feature generally enhances its solubility in polar solvents.
  • Common Solvents: It is typically soluble in solvents such as water, alcohols, and acetone. However, its solubility may vary significantly depending on temperature and concentration.
  • Temperature Effects: Like many organic compounds, solubility can increase with temperature. This is an important consideration when preparing solutions for laboratory use or in industrial applications.
  • Applications Impact: The solubility profile contributes to its efficacy in agricultural chemistry, particularly as a pesticide or herbicide, as well as in pharmaceutical formulations.

Overall, understanding the solubility of 2-methylallyl carbamate is crucial for optimizing its effectiveness in various chemical processes and applications. Being aware of its solubility helps chemists manipulate its use efficiently in synthetic methods and product formulations.

Interesting facts

Interesting Facts about 2-Methylallyl Carbamate

2-Methylallyl carbamate is a fascinating chemical compound with diverse applications and properties that intrigue both scientists and industry experts alike. Here are some interesting insights about this compound:

  • Versatile Use: 2-Methylallyl carbamate is primarily known for its role in the synthesis of various pharmaceuticals and agrochemicals, making it significant in the field of medicinal and agricultural chemistry.
  • Structure and Reactivity: The unique molecular structure of 2-methylallyl carbamate allows it to participate in several organic reactions. Its reactivity can be harnessed to develop novel derivatives, expanding its utility in synthetic methodologies.
  • Biochemical Activity: Researchers have observed that carbamates such as 2-methylallyl carbamate can exhibit interesting biochemical properties, which can lead to potential therapeutic effects. This opens up avenues for further studies in drug development.
  • Environmental Considerations: As with many carbamates, understanding the environmental impact of 2-methylallyl carbamate is crucial. Studies on its degradation and potential toxicity are vital to ensure safe usage in agricultural practices.
  • Historical Significance: Carbamates have a long history of use, dating back to the early 19th century, and 2-methylallyl carbamate contributes to this rich legacy through its molecular versatility and the innovations it inspires.

Overall, the exploration of 2-methylallyl carbamate showcases the intricate relationship between chemistry and its applications. As researchers continue to delve into its properties, there is the potential for new discoveries that could impact various fields, from medicine to environmental science.

"Chemistry is the study of transformation." – Unknown This quote reminds us of the transformative potential that compounds like 2-methylallyl carbamate can hold!

Synonyms
Methallyl carbamate
CARBAMIC ACID, 2-METHYLALLYL ESTER
0CB506VO6N
2-Methyl-2-propen-1-ol carbamate
NSC 66325
NSC-66325
2-Propen-1-ol, 2-methyl-, carbamate
BRN 2959681
UNII-0CB506VO6N
AI3-02681
DTXSID10175379
2-PROPEN-1-OL, 2-METHYL-, 1-CARBAMATE
2-Propen-1-ol, 2-methyl-, carbamate (8CI,9CI)
DTXCID5097870
654-647-4
2114-14-9
2-methylprop-2-enyl carbamate
(2-methylprop-2-en-1-yl) carbamate
2-Methylallyl carbamate
2-Propen-1-ol, carbamate
NCIOpen2_000070
SCHEMBL9445541
MNPKKYZUEZVQNJ-UHFFFAOYSA-N
NSC66325
AKOS006342745